Canonical Allele Identifier: CA587804373

Gene: GRHPR

Linked Data

• dbSNP Id: rs1564300195
• gnomAD v2: 9-37429716-CT-C
• gnomAD v4: 9-37429719-CT-C
• MyVariant Identifiers: chr9:g.37429717del (hg19) ; chr9:g.37429720del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429720del , CM000671.2:g.37429720del	GRCh38
NC_000009.11:g.37429717del , CM000671.1:g.37429717del	GRCh37
NC_000009.10:g.37419717del	NCBI36
NG_008135.1:g.12011del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-12del MANE Select	ENSP00000313432.6:n.494-12del
ENST00000318158.10:c.494-12del	ENSP00000313432.6:n.494-12del
ENST00000377824.8:n.531-12del
ENST00000460882.5:n.521-12del
ENST00000480596.5:n.1183del
ENST00000491488.5:n.199-12del
ENST00000494290.1:c.53del	ENSP00000432021.1:p.Leu18ProfsTer4
ENST00000497693.1:n.2015del
ENST00000607784.1:c.494-12del	ENSP00000475569.1:n.494-12del
NM_012203.1:c.494-12del	NP_036335.1:n.494-12del
XM_005251631.1:c.173-12del	XP_005251688.1:n.173-12del
XM_011518073.1:c.92-12del	XP_011516375.1:n.92-12del
XR_929374.1:n.939-12del
XM_017015320.2:c.494-12del	XP_016870809.1:n.494-12del
XM_017015321.2:c.494-12del	XP_016870810.1:n.494-12del
XM_017015323.2:c.92-12del	XP_016870812.1:n.92-12del
XM_024447716.1:c.767-12del	XP_024303484.1:n.767-12del
XM_024447717.1:c.767-12del	XP_024303485.1:n.767-12del
XR_002956828.1:n.782-12del
XR_002956829.1:n.782-12del
XR_002956830.1:n.553-12del
XR_002956831.1:n.228-12del
XR_002956832.1:n.913-12del
NM_012203.2:c.494-12del MANE Select	NP_036335.1:n.494-12del